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HRID 580604作成日:2026年10月25日

Water → 4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholide

https://huagongshe.com/reaction/580604

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物Phosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl esterHCID 11207805—
反応物4-Amino-3,4',5-trichlorobenzophenoneHCID 13373314—
溶媒TetrahydrofuranHCID 8028—
生成物4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholideHCID 54521919—

反応手順

A solution of 5.3 g (0.02 mol) of diethylphosphonoacetic acid morpholide in 100 ml of dry tetrahydrofuran was slowly added dropwise, while stirring, to a suspension of 1 g of sodium hydride (0.02 mol, 50% in oil) in 50 ml of dry tetrahydrofuran. Slight heating and strong foaming occurred. After all had been added, the mixture was stirred for 10 minutes more. A solution of 3 g (0.01 mol) of 4-amino-3,4',5-trichlorobenzophenone in 20 ml of dry tetrahydrofuran was added dropwise to the resulting clear solution, and the mixture was heated for 16 hours at reflux temperature. After cooling, the solution was poured into water, and the aqueous mixture was extracted exhaustively with methylene chloride. The methylene chloride phase was dried with sodium sulfate and evaporated by evaporation in vacuo. The residue was crystallized from isopropanol/petroleum ether. The colorless crystals thus obtained, melting point 150°-155° C., contained the cis/trans isomers in a ratio of 1:3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04753934
出典データセットuspto-grants-1988_06
ORD IDord-d3a7eb78bd444d0fb967eeb28ced0d84
出典メモuspto-grants-1988_06